2-Aminoindan hydrochloride

2-Aminoindan hydrochloride Basic information

Product Name:	2-Aminoindan hydrochloride
Synonyms:	2,3-dihydro-1h-inden-2-aminehydrochloride;1H-Inden-2-aMine,2,3-dihydro-, hydrochloride (1:1);Indan-2-ylamine hydrochloride;2-AMINOINDANE HYDROCHLORIDE;2-AMINOINDAN HYDROCHLORIDE;2-INDANAMINE HCL;2-INDANAMINE HYDROCHLORIDE;2,3-DIHYDRO-1H-INDEN-2-AMINE HCL
CAS:	2338-18-3
MF:	C9H12ClN
MW:	169.65128
EINECS:	219-048-0
Product Categories:
Mol File:	2338-18-3.mol

2-Aminoindan hydrochloride Chemical Properties

Melting point	245-247 °C(lit.)
storage temp.	-20°C Freezer, Under Inert Atmosphere
solubility	DMSO (Slightly), Methanol (Slightly)
form	Solid
color	White to Off-White
BRN	3913700
CAS DataBase Reference	2338-18-3(CAS DataBase Reference)

Safety Information

Hazard Codes	Xn
Risk Statements	22
Safety Statements	22-24/25
WGK Germany	3
RTECS	NK4050000
HS Code	29214990
Toxicity	dog,LDLo,oral,50mg/kg (50mg/kg),BEHAVIORAL: ANALGESIA,Journal of Pharmacology and Experimental Therapeutics. Vol. 133, Pg. 400, 1961.

MSDS Information

2-Aminoindan hydrochloride Usage And Synthesis

Description	Aminoindans (AI) were originally studied as semi-rigid congeners of phenylethylamines, which are psychoactive alkaloids. 2-AI is an aminoindane that serves as the starting point for the synthesis of psychoactive compounds, such as 5,6-methylenedioxy-2-aminoindane. 2-AI itself has modest analgesic and stimulatory properties. This product is intended for forensic applications.
Chemical Properties	White powder
Uses	Prepared from 2-indanols via azide displacement and subsequent hydrogenation.
References	[1] JOSEPH G. CANNON. Comparison of biological effects of N-alkylated congeners of .beta.-phenethylamine derived from 2-aminotetralin, 2-aminoindan, and 6-aminobenzocycloheptene[J]. Journal of Medicinal Chemistry, 1980, 23 7: 745-749. DOI: 10.1021/jm00181a009

2-Aminoindan hydrochloride Preparation Products And Raw materials

Raw materials	Carbamic acid, (2,3-dihydro-1H-inden-2-yl)-, ethyl ester (9CI)-->2-azido-2,3-dihydro-1h-indene-->INDAN-1,2-DIONE-2-OXIME-->2-Indanone oxime-->2-Indanol-->p-Anisaldehyde-->Ninhydrin hydrate-->1-Indanone
Preparation Products	Indan-2-amine

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